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9,882 results for “Scale”
Figure 3. Crypticerya multicicatrices. A in Report of new invasive scale insects (Hemiptera: Coccoidea), Crypticerya multicicatrices Kondo and Unruh (Monophlebidae) and Maconellicoccus hirsutus (Green) (Pseudococcidae), on the islands of San Andres and Providencia, Colombia, with an updated taxonomic key to iceryine scale insects of South America
Figure 3. Crypticerya multicicatrices. A. On Cajanus cajan. B. On Spondias purpurea. C. On Tectona grandis. D. On Citrus latifolia. E. On Delonix regia. F. On a palm. G. On Carica papaya. H. On Artocarpus altilis. Notice sooty mold on leaves. I. Dieback of Erythrina variegata street trees.
Figure 3 in Updated list of Pinnaspis armored scales (Hemiptera: Diaspididae) of Korea
Figure 3.Three species of Pinnaspis. A) P. uniloba (Kuwana), female. B) P. uniloba (Kuwana), antennae. C) P. uniloba (Kuwana), anterior and posterior spiracles. D) P. uniloba (Kuwana), median lobes and preanal scars. E) P. uniloba (Kuwana), perivulvar pores. F) Slide-mounted specimens.
Figure 2. Pinnaspis hikosana Takagi. A in Updated list of Pinnaspis armored scales (Hemiptera: Diaspididae) of Korea
Figure 2. Pinnaspis hikosana Takagi. A) Habitus. B) Female. C) Antennae. D) Anterior and posterior spiracles. E) Median lobes and preanal scars. F) Perivulvar pores.
Figure 1. Pinnaspis chamaecyparidis Takagi. A in Updated list of Pinnaspis armored scales (Hemiptera: Diaspididae) of Korea
Figure 1. Pinnaspis chamaecyparidis Takagi. A) Habitus. B) Female. C) Antennae. D) Anterior and posterior spiracles. E) Median lobes. F) Perivulvar pores.
Figures 1–9 in New records of Chionaspis armored scales (Hemiptera: Diaspididae) in Korea
Figures 1–9. Habitus and structures of two species of Chionaspis. 1–3: Chionaspis acer (Takagi and Kawai), 1) female, 2) pygidium (bark-infesting form), 3) anterior spiracle. 4–9: Chionaspis wistariae Cooley, 4–5) habitus, 6) female, 7) pygidium of leaf-infesting form with median lobes sunken into the apex of pygidium, 8) pygidium of bark-infesting form with median lobes appressed medially, 9) anterior spiracle.
Figures 1–9 in Scale insects (Hemiptera: Coccoidea) found on dracaena and ficus plants (Asparagales: Asparagaceae, Rosales: Moraceae) from southeastern Asia
Figures 1–9. Some scale insects collected on dracaena and ficus plants in Cambodia, Laos, Thailand and Vietnam. 1) Drepanococcus chiton (Green). 2) Paralecanium quadratum (Green). 3) Parasaissetia nigra (Nietner). 4) Fiorinia coronata Williams and Watson. 5) Gymnaspis ficus Ramakrishna Ayyar. 6) Unaspis acuminata (Green). 7) Dysmicoccus neobrevipes Beardsley. 8) Ferrisia virgata (Cockerell). 9) Rhizoecus americanus (Hambleton).
Figure 1. The white coconut scale, Parlagena bennetti. A in New distribution and host records for white coconut scale, Parlagena bennetti Williams (Hemiptera: Diaspididae)
Figure 1. The white coconut scale, Parlagena bennetti. A). Infesting coconut fruits. B). Close-up of insects infesting fruit. C). Typical infestation on leaves. Photographs by T. Kondo, Palmira, Colombia.
Figure 2. A in New distribution and host records for white coconut scale, Parlagena bennetti Williams (Hemiptera: Diaspididae)
Figure 2. A). Auto-montage photomicrograph of an adult female of Parlagena bennetti from Venezuela, Lara, Barquisimeto. Photomicrograph by G.W. Watson, California Department of Food & Agriculture. B). Illustration of body and details of the pygidium (after Williams 1969).
Figures 9–17 in Geographical distribution and phenotypic variation of Anovia punica Gordon (Coleoptera: Coccinellidae: Noviini), a predatory ladybeetle of fluted scales (Hemiptera: Coccoidea: Monophlebidae)
Figures 9–17. Male genitalia of Anovia punica. Peru: 9–11) San Martin State. Colombia: 12–14) San Andres Island. 15–17) Magdalena State. 9), 12), 15) Tegmen in ventral view. 10), 13), 16) Tegmen in lateral view. 11), 14), 17) Sipho.
Figures 1–8 in Geographical distribution and phenotypic variation of Anovia punica Gordon (Coleoptera: Coccinellidae: Noviini), a predatory ladybeetle of fluted scales (Hemiptera: Coccoidea: Monophlebidae)
Figures 1–8. Morphological variation of Anovia punica. Peru. 1–2) San Martín State. Colombia: 3) San Andres Island. 4) Magdalena State. 5) Valle del Cauca State. 6–7) Antioquia State. 8) Atlantico State.
Data for the manuscript entitled "Factors driving large-scale ungulate carrion production in the Anthropocene"
<p>Data for the article entitled "Factors driving large-scale ungulate carrion production in the Anthropocene". The data includes 5 main datasets, each of those corresponding to 5 main carrion production sources in terrestrial ecosystems in peninsular Spain, namely; 1) Livestock, 2) Big Game Hunting, 3) Roadkills, 4) Predation and 5) Natural mortality. </p> <p>In case of any doubt/s or enquiries regarding this data, please, send an email to the corresponding author; Jon Morant Etxebarria (email: jmorant@aranzadi.eus). </p> <p> </p>
Centennial scale climate oscillations from southern Siberia in the Last Glacial Maximum
<p>A lack of adequate high resolution climate proxy records for the Last Glacial Maximum (LGM) has prevented the extrapolation of climate–solar linkages on centennial time scales prior of the Holocene. Therefore, it is still unknown whether centennial climate variations of the last ten thousand years convey a universal climate change or merely represent a characteristic of the Holocene. Recently published high resolution climate proxy records for the LGM allowed us to extrapolate climate–solar linkages on centennial time scales ahead of the Holocene. Here we present the analysis of a high resolution pollen concentration record from Lake Kotokel in southern Siberia, Russia, during the LGM. The record reflects the dynamics of vegetation zones and temperature change with a resolution of ~ 40 years in the continental climate of north-eastern Asia. We demonstrate that our pollen concentration record, the oxygen isotope δ<sup>18</sup>O record from the Greenland ice core project NGRIP (NorthGRIP), the dust-fall contributions in Lake Qinghai, China, grain size in the Gulang and Jingyuan loess deposits, China, and the composite oxygen isotope δ<sup>18</sup>O record from the Alpine cave system 7H reveal cooler to warmer climate fluctuations between ~ 20.6 and 26 ka. Such fluctuations correspond to the ~ 1000-yr, 500-600-yr and 210-250-yr cycles possibly linked to the solar activity variations and recognized in high resolution Holocene proxies all over the world. We further show that climate fluctuations in the LGM and Holocene are spectrally similar suggesting that linkages between climate proxies and solar activity at the centennial time scale in the Holocene can be extended to the LGM.</p>
Datasets for the manuscript "In silico proof of principle of machine learning-based antibody design at unconstrained scale"
<p>The zip file contains dataset files for the manuscript "In silico proof of principle of machine learning-based antibody design at unconstrained scale"</p>
Figure 6 in Microstructures and nanostructures of high Andean Penaincisalia lycaenid butterfly scales (Lepidoptera: Lycaenidae): descriptions and interpretations
Figure 6. Scanning electron micrographs of Thecloxurina atymna scale microstructures. (A) Tile- or shovel-shaped scales, deep dentation; (B) low longitudinal ridges with flutes, straight cross ribs, and rectangular microcells; (C–F) strong ridges and ribs in slight disorder, microcells open or closed; (G, H) wispy material in microcells.
Figure 7 in Microstructures and nanostructures of high Andean Penaincisalia lycaenid butterfly scales (Lepidoptera: Lycaenidae): descriptions and interpretations
Figure 7. Illustration showing the principle of regular, three-dimensional arrangement of two materials with different indexes of refraction, n1 and n2.
Figure 1 in Microstructures and nanostructures of high Andean Penaincisalia lycaenid butterfly scales (Lepidoptera: Lycaenidae): descriptions and interpretations
Figure 1. Lycaenid butterfly species investigated showing male dorsal wing surfaces. (A) Penaincisalia aurulenta Johnson, 1990 (Peru: PN Huascarán, Quebrada Demanda; HNHM); (B) Penaincisalia perezi Bálint, 2001 (Peru: PN Husacarán; Llanganuco; HNHM paratype); (C) Penaincisalia culminicola (Staudinger, 1894) (Peru: PNB Huascarán, Llanganuco; HNHM); (D) Thecloxurina loxurina (Felder and Felder, 1865) (Ecuador: Carchi, Res. Forest. Golondrinas; HNHM); (E) Thecloxurina atymna (Hewitson, 1870) (Ecuador: Zamora, Cord. Lagunillas; HNHM); (F) Thecloxurina atymna (Hewitson, 1870) (Ecuador: Azuay, Cuenca; HNHM).
Figure 2 in Microstructures and nanostructures of high Andean Penaincisalia lycaenid butterfly scales (Lepidoptera: Lycaenidae): descriptions and interpretations
Figure 2. Scanning electron micrographs of Penaincisalia aurulenta scale microstructures. (A) Tile- and shovelshaped scales with dentate anterior margins; (B) longitudinal ridges with flutes, straight cross ribs; (C) widely open microcells, wispy internal structures; (D) widely open microcells, deep-laying pepper-pot structures.
Figure 5 in Microstructures and nanostructures of high Andean Penaincisalia lycaenid butterfly scales (Lepidoptera: Lycaenidae): descriptions and interpretations
Figure 5. Scanning electron micrographs of Thecloxurina loxurina scale microstructures. (A) Tile- or shovel-shaped scales with anterior dentation; (B) no anterior dentation; (C) moderate longitudinal ridges with flutes, curved cross ribs, pepper-pot layers; (D) deep-laying pepper-pot layers; (E) high longitudinal ridges, very closely set v-shaped cross ribs; (F) microcells with small circular opening in abyss.
Figure 3 in Microstructures and nanostructures of high Andean Penaincisalia lycaenid butterfly scales (Lepidoptera: Lycaenidae): descriptions and interpretations
Figure 3. Scanning electron micrographs of Penaincisalia perezi scale microstructures. (A) Tile- and shovel-shaped scales with dentate anterior margins; (B) low longitudinal ridges with flutes, straight cross ribs, open microcells, deep-laying pepper-pot structures; (C) moderate longitudinal ridges, curved cross-ribs, pepper-pot layers; (D) high longitudinal ridges, v-shaped cross ribs, small circular opening in microcell abyss.
Figure 6 in Comparative morphology of scales of four teleost fishes from Sudan and Yemen
Figure 6. Scales from different body regions of Lates niloticus. (A–H) Regions 1–8; (I) area around anus; (J) lateral line scale. Scale bars: 1 mm.
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.